Cytovale
At Cytovale, we’re focused on more rapid and insightful ways to diagnose fast-moving and immune-mediated diseases.
medical device
51 - 200
Quality Engineer II
August 26
🏢 In-office - San Francisco
Cytovale
At Cytovale, we’re focused on more rapid and insightful ways to diagnose fast-moving and immune-mediated diseases.
medical device
51 - 200
Description
• Key member of the Quality Assurance team responsible for process and product performance quality • Support process validation and manufacturing process improvements • Interface with cross-functional partners on new product development and design/process change control • Monitor quality performance metrics and drive corrective/preventive actions
Requirements
• Bachelor’s degree in scientific discipline (e.g. Engineering, Life Sciences, etc) • 3+ years related experience in the medical device industry • Proficiency with Microsoft Office (e.g., Word, Excel, Project, etc) • Knowledge of regulations and standards such as 21 CFR 820, ISO 13485, ISO 14971, etc • Prior experience with QMS processes such as Document Control, Materials Control, Receiving, CAPAs, NCRs, Training, etc. required • Good organizational skills as well as strong written/verbal communications skills
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